Overview

Dexmedetomidine for Cesarean Section

Status:
Completed
Trial end date:
2015-11-01
Target enrollment:
0
Participant gender:
Female
Summary
Current cesarean section often chooses spinal anesthesia. And in order to avoid the impact of drugs on the fetus, before the delivery, anesthesiologist generally don't use sedative or analgesic drugs. However, the majority of puerperas would appear nervous, anxiety, fear and other psychological reactions in cesarean section. Although the placental transfer and the foetal metabolism of dexmedetomidine have been reported and the result show no adverse effects on neonates, but the placental transfer of dexmedetomidine in intravertebral anesthesia area was lack of systematical research. This study intends to use of dexmedetomidine in the cesarean section under epidural anesthesia and investigate its effects on the parturients' haemodynamics and the neonates' placental transfer and metabolism.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
The First Affiliated Hospital with Nanjing Medical University
Treatments:
Dexmedetomidine
Criteria
Inclusion Criteria:

- 40 cases of full-term puerperas with single baby ASA I or II, aged 23 to 41 years old,
weighing 61-92 kg, without spinal canal puncture contraindication and scheduled for
caesarean section under epidural anesthesia were selected for this study.

Exclusion Criteria:

- women with a history of cardiac, liver, or kidney diseases;

- women with allergy to amide local anesthetics;

- women with epilepsy;

- those taking cardiovascular medications;

- those with pregnancy-induced hypertension;

- women with evidence of intrauterine growth restriction or fetal compromise.